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Heart Block clinical trials

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NCT ID: NCT05015660 Recruiting - Pacemaker DDD Clinical Trials

Conduction System Pacing With Left Bundle Branch Pacing as Compared to Standard Right Ventricular Pacing

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

High burden right ventricular (RV) pacing has been shown to increase cardiovascular mortality, incidence of heart failure (HF), worsen left ventricular (LV) function and accelerate the development of atrial fibrillation (AF). High percentage ventricular pacing and wider paced QRS in the setting of normal baseline LV ejection fractions have consistently been shown to be independent risk factors for pacing-induced cardiomyopathy. Left bundle branch pacing (LBBP) has emerged as a potential alternative pacing mechanism that may avoid LV dyssynchrony and pacing-induced LV dysfunction by mimicking native electrical conduction.

NCT ID: NCT04982406 Recruiting - Aortic Stenosis Clinical Trials

Transcatheter Aortic Valve Replacement (TAVR) Effects on Cardiac Conduction System

TAVR-HBE
Start date: May 18, 2021
Phase:
Study type: Observational [Patient Registry]

This is a prospective observational study, the purpose of which is to: 1. Characterize response of the AV conduction system to TAVR with various prostheses by recording continuous His bundle electrograms during valve placement. 2. Correlate preprocedure ECG features with changes in AV nodal and infranodal conduction during placement of the valve prosthesis. 3. Correlate changes in AV nodal and infranodal conduction during the procedure with risk of developing AV conduction block after TAVR. 4. Assess the contribution of stressing the conduction system by atrial pacing prior to and following TAVR to prediction of postprocedural heart block. Assess the correlation between new onset bundle branch block, site and degree of conduction block or delay and subsequent development of high-grade or complete AV block.

NCT ID: NCT04559425 Recruiting - Clinical trials for Heart Block Second Degree

Slow Heart Registry of Fetal Immune-mediated High Degree Heart Block

Start date: January 1, 2020
Phase:
Study type: Observational [Patient Registry]

Few studies are specifically designed to address health concerns that are already relevant during pregnancy. The consequence is a lack of evidence on best clinical practice. This includes mothers and their babies when pregnancy is complicated by an abnormally slow heart rate due to maternal antibody-mediated heart disease in the unborn baby (fetus). Since the late seventies, it has been possible to detect and monitor fetal disease by ultrasound images and to treat selected conditions with pharmaceuticals administered via the mother. To this day, physicians need to make decisions about the management of such pregnancies without evidence from prospective clinical trials on drug efficacy and safety. The SLOW HEART REGISTRY is a multi-centered prospective observational study that will address the knowledge gap to guide future management of high-degree immune-mediated heart block to the best of care. The study seeks to establish an international database of the management and outcome of affected fetuses, to be used to publish information on the results of currently available prenatal care and to evaluate the need for additional research.

NCT ID: NCT04409119 Recruiting - Heart Failure Clinical Trials

Direct HIS/LBB Pacing as an Alternative to Biventricular Pacing in Patients With HFrEF and a Typical LBBB.

HIS-alt_2
Start date: June 1, 2020
Phase: N/A
Study type: Interventional

The study will investigate the feasibility of using direct HIS pacing or left bundle branch pacing (LBB pacing) as an alternative to biventricular pacing in patients with symptomatic heart failure and an ECG with a typical left bundle branch block pattern.

NCT ID: NCT04293471 Recruiting - Clinical trials for Left Bundle-Branch Block

Prediction of Outcome by Echocardiography in Left Bundle Branch Block

EchoLBBB
Start date: April 15, 2021
Phase:
Study type: Observational [Patient Registry]

Patients with left bundle branch block have an increased risk for the development of heart-failure and death. However, risk factors for unfavorable outcomes are still poorly defined. This study aims to identify echocardiographic parameters and ECG characteristics by machine learning in order to develop individual risk assessment

NCT ID: NCT04128384 Recruiting - Clinical trials for Left Bundle-Branch Block

Infranodal Conduction Time During TAVR as Predictor of HAVB

HOM-TAVI
Start date: June 21, 2018
Phase: N/A
Study type: Interventional

Consecutive patients with high grade aortic stenosis undergoing transcatheter aortic valve replacement (TAVR) with a self-expanding valve (Medtronic CoreValve Evolut R® or Edwards Sapien S3®) without pre-existing pacemaker devices are eligible for inclusion. During the TAVR procedure, an electrophysiologic study including measurements of infranodal conduction times (HV-interval before and after valve implantation) will be performed. Electrocardiograms before TAVR, before discharge, after 30 days and after 12 months will be analyzed regarding new onset LBB and the occurrence of high-degree AV block (HAVB) .

NCT ID: NCT03096678 Recruiting - Cardiac Failure Clinical Trials

Prognosis of Patients With Compete Left Bundle Branch Block

Start date: January 1, 2010
Phase: N/A
Study type: Observational [Patient Registry]

The investigators sought to evaluate the morphological and functional changes, risk stratification and prognosis of patients of participants with compete left bundle branch block (CLBBB). The conduction of this study was largely due to the increased clinical requirement, which reflected the increased awareness among physicians of heart failure due to asynchronous cardiac function caused by CLBBB. The investigators also aim to figure out the time point or CMR parameters for cardiac resynchronization therapy in patients with CLBBB.

NCT ID: NCT02881671 Recruiting - Clinical trials for Congenital Complete Heart Block

Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms

Start date: January 2011
Phase:
Study type: Observational

Identification of genes involved in congenital atrioventricular block and progressive Cardiac Conduction Disease.

NCT ID: NCT02637362 Recruiting - Hallux Valgus Clinical Trials

Optimal Analgesia for Forefoot Surgery

Start date: February 2, 2018
Phase: N/A
Study type: Interventional

A randomised trial comparing three analgesic strategies for patients undergoing forefoot surgery in a day-surgery setting.

NCT ID: NCT01829126 Recruiting - Clinical trials for Congestive Heart Failure

Development and Prevention of Severe Heart Disease in Systemic Sclerosis

Start date: April 2013
Phase: N/A
Study type: Observational [Patient Registry]

Systemic sclerosis is an orphan, multiorgan disease affecting the connective tissue of the skin and all internal organs. Cardiac involvement, mainly characterised by small intramyocardial coronary artery involvement and myocardial fibrosis, can cause the development of impaired diastolic ventricular filling, cardiac blocks and ventricular arrhythmias, and can ensue in congestive heart failure and sudden death. Until now, no drug has been proven to have a therapeutic effect on SSc myocardial disease on an evidence-based level. Short-term trials and retrospective studies have suggested a favourable and protective effect of calcium channel blockers and angiotensin converting enzyme inhibitors in patients with myocardial involvement. However, no data are presently available on the prevention and treatment of severe heart disease. This observational trial is part of the collaborative project "DeSScipher", one out of five observational trials to decipher the optimal management of systemic sclerosis. Aim of this observational trial is to assess the efficacy and safety of calcium channel blockers and angiotensin converting enzyme inhibitors in asymptomatic SSc patients with cardiac involvement.